EP0563372B1 - Vollkeramische dentalprothese aus aluminiumoxyd/magnesiumoxyd spinell enthaltend keramik und verfahren zu seiner herstellung - Google Patents

Vollkeramische dentalprothese aus aluminiumoxyd/magnesiumoxyd spinell enthaltend keramik und verfahren zu seiner herstellung Download PDF

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Publication number
EP0563372B1
EP0563372B1 EP92923838A EP92923838A EP0563372B1 EP 0563372 B1 EP0563372 B1 EP 0563372B1 EP 92923838 A EP92923838 A EP 92923838A EP 92923838 A EP92923838 A EP 92923838A EP 0563372 B1 EP0563372 B1 EP 0563372B1
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Prior art keywords
alumina
paste
prosthesis
weight
magnesia
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EP92923838A
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English (en)
French (fr)
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EP0563372A1 (de
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Michèle Tyszblat
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C13/00—Dental prostheses; Making same
    • A61C13/0003—Making bridge-work, inlays, implants or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00—Preparations for dentistry
    • A61K6/15—Compositions characterised by their physical properties
    • A61K6/17—Particle size
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00—Preparations for dentistry
    • A61K6/70—Preparations for dentistry comprising inorganic additives
    • A61K6/78—Pigments
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00—Preparations for dentistry
    • A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
    • A61K6/802—Preparations for artificial teeth, for filling teeth or for capping teeth comprising ceramics
    • A61K6/807—Preparations for artificial teeth, for filling teeth or for capping teeth comprising ceramics comprising magnesium oxide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00—Preparations for dentistry
    • A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
    • A61K6/802—Preparations for artificial teeth, for filling teeth or for capping teeth comprising ceramics
    • A61K6/816—Preparations for artificial teeth, for filling teeth or for capping teeth comprising ceramics comprising titanium oxide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00—Preparations for dentistry
    • A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
    • A61K6/802—Preparations for artificial teeth, for filling teeth or for capping teeth comprising ceramics
    • A61K6/824—Preparations for artificial teeth, for filling teeth or for capping teeth comprising ceramics comprising transition metal oxides

Definitions

  • the present invention relates to a fully ceramic translucent dental prosthesis based on alumina / magnesia spinel, as well as its manufacturing process.
  • European patent application 0 030 851 also discloses non-shrinking ceramic prostheses containing spinels of aluminum oxide and magnesium oxide, but these prostheses also contain a high content of silicon oxide, so that 'they have no translucency, which makes them look very different from natural teeth.
  • the present invention relates to translucent dental prostheses obtained by infiltration of a glass into the pores of a solid infrastructure and whose infrastructure made from alumina / magnesia spinel can be shaped either directly in the mouth by the dentist, or on a model of the tooth by the prosthetist.
  • the prostheses according to the invention have the advantage of being entirely ceramic, of being translucent like the enamel of natural teeth, of being weakly colored or not colored if desired, and of having a high mechanical resistance while by being perfectly biocompatible.
  • the dental prostheses according to the invention can advantageously but not limited to be used to produce parts known under the names of "inlay” and “onlay” or crowns.
  • the subject of the present invention is a process for manufacturing ceramic dental prostheses, translucent like tooth enamel, having high mechanical strength and which are biocompatible, this process being characterized by the fact that a plastic paste is produced by a mixture of organic resin or binder with fine particles of alumina / magnesia spinel, alumina and magnesia; that said paste is given the shape that the prosthesis should have; that one causes the polymerization of the resin or the setting of the binder to fix the shape of the paste; that the dough thus formed is subjected to a heat treatment to initially cause the calcination of the resin or of the binder and then reactive sintering of the alumina / magnesia spinel, alumina and magnesia particles; that one possibly proceeds to the rectification of the shape of the porous infrastructure thus obtained; and that this infiltration of this infrastructure is carried out using a molten glass.
  • the spinel used according to the invention is the spinel formed from quantities close to the stoichiometric composition of aluminum oxide or alumina (Al2O3) and of magnesium oxide or magnesia (MgO).
  • this spinel will be designated by the expression "MgAl2O4 spinel” or alumina / magnesia spinel.
  • the reactive sintering during which the alumina and the magnesia which, according to the invention, are added to the spinel MgAl2O4 combines at least partially to produce an additional quantity of spinel MgAl2O4.
  • This reaction leads to an expansion of the volume of the porous infrastructure which corresponds, depending on the sintering heat treatment and the amount of additional spinel formed which can be between 0.6 and 4% of variation in linear dimension.
  • This expansion makes it possible to exactly compensate for the retraction of the paste which occurs during the polymerization of the resin or the setting of the binder, retraction which can correspond for example to a reduction in linear dimension of 0.1 to 2%, as well as the shrinkage due to the calcination of the resin or of the binder which may correspond, for example, to a reduction in linear dimension of 0.5 to 2%.
  • the mineral filler which is introduced into the paste to which the shape of the prosthesis is given comprises, apart from the spinel, additions of alumina and magnesia which, in combining during reactive sintering, expand to compensate for the shrinkage resulting from the polymerization of the resin or the setting of the binder and then from their calcination.
  • the polymerizable resin which can be used in the paste is an organic resin which is destroyed during its calcination, such as resins of the polyepoxide, polyester or vinyl ester type.
  • the organic binder which is also usable in the pulp can be a cellulose ester such as methyl cellulose, methylhydroxyethyl cellulose, methylhydroxypropyl cellulose, carboxymethyl cellulose, or hydroxyethyl cellulose or sodium or ammonium alginate, all products which are soluble in water.
  • a cellulose ester such as methyl cellulose, methylhydroxyethyl cellulose, methylhydroxypropyl cellulose, carboxymethyl cellulose, or hydroxyethyl cellulose or sodium or ammonium alginate, all products which are soluble in water.
  • the organic binder can also be a cellulose ether such as ethyl cellulose or acetate cellulose or alternatively polyvinyl butyral which are soluble in organic solvents.
  • a cellulose ether such as ethyl cellulose or acetate cellulose or alternatively polyvinyl butyral which are soluble in organic solvents.
  • the resin or the binder must as far as possible not contain any compound such as silica which does not disappear during the calcination. Indeed, such compounds have the effect of making the prosthesis lose its translucent character which characterizes the prostheses according to the invention.
  • the mineral filler of the paste consists of a mixture of fine particles comprising by weight from 50 to 84% of spinel MgAl2O4, from 10 to 32% of alumina and from 6 to 18% magnesia.
  • These particles preferably have a particle size less than 40 microns and advantageously between 0.5 and 20 microns.
  • the polymerizable resin as defined above, in which the mineral filler can be incorporated for example comprises by weight 40 to 90% of poly-epoxy, polyester or vinyl ester resin, 0 to 80% of reactive diluent monomer, 0, 5 to 5% of catalyst, 0 to 4% of accelerator and 0 to 10% of plasticizer.
  • the organic binder as defined above, in which the mineral filler can be incorporated may for example comprise from 3 to 15% by weight of organic binder, up to 10% by weight of plasticizer and from 75 to 95% by weight of water or organic solvent.
  • the paste to which the shape of the prosthesis is given advantageously contains from 55 to 78% by volume of metal oxides, the rest being constituted by the resin or the binder defined above.
  • the paste thus obtained can be used directly by the dentist who applies it to the previously prepared tooth which must receive the prosthesis and gives it the shape which the prosthesis must have.
  • the binder sets in the mouth while the resin undergoes photopolymerization in the mouth, then, after demolding, thermopolymerization.
  • the resin undergoes chemopolymerization in the mouth, that is to say a chemical polymerization.
  • a porous ceramic shell which is easily machinable.
  • a porous ceramic shell can consist of 70 to 100% by weight of MgAl2O4 spinel, up to 30% by weight of whiskeys such as alumina, magnesia or mullite (3Al2O3-2SiO2) and up to 20 % by weight of alumina or silica fibers.
  • this composition is subjected to sintering from 1200 to 1400 ° C. It then has an open porosity of 10 to 30% by volume.
  • This shell will constitute the external surface of the prosthesis, which greatly facilitates and simplifies the shaping of the paste by the dentist to produce the infrastructure.
  • this shaping is carried out by taking the traditional impressions which are used for the manufacture of prostheses.
  • the sintering of the blank thus obtained is carried out for example in an air oven by firstly causing the calcination of the resin or of the binder by raising the temperature to 4/500 ° C. in 1 to 8 hours. According to the invention, this calcination is carried out while leaving a minimum of solid residue.
  • the temperature is brought to around 1050/1200 ° C in 1 hour, then it is kept constant for for example 1 to 4 hours to cause sintering.
  • infiltration of the porous infrastructure is carried out by a glass brought to the liquid state at high temperature.
  • This infiltration is carried out for example by placing the porous infrastructure in a cup on the glass powder by raising the temperature to air at 6/700 ° C. in 3 to 10 minutes then under vacuum, bringing the temperature to 1100 / 1200 ° C in 10 to 60 minutes, after which the temperature is maintained under vacuum at a level for for example 20 minutes to 2 hours.
  • the glass can advantageously consist of a mixture of 12 to 30% of silica (SiO2), of 3 to 20% of alumina (Al2O3), of 3 to 20% of boron oxide (B2O3), of 15 to 45 % of lanthanum oxide (La2O3), from 0 15%, yttrium oxide (Y2O3), 0 to 8% titanium oxide (TiO2) and 0 to 4% coloring oxides.
  • the excess glass is removed by sandblasting.
  • the present invention also relates to a ceramic, biocompatible dental prosthesis, having a translucency similar to that of the teeth as well as good mechanical strength, characterized in that it was obtained by the process described above and that it consists of a rigid porous infrastructure obtained by reactive sintering of fine particles of alumina / magnesia spinel, alumina and magnesia, the pores of said structure being occupied by glass subsequently infiltrated at high temperature.
  • the overall composition by weight of the ceramic prosthesis according to the invention can for example be as follows: Spinel MgAl2O4 45 to 70% Alumina 8 to 20% Magnesia 3 to 12% Glass 20 to 40%
  • the prosthesis according to the invention can advantageously be enamelled in volume with a ceramic whose coefficient of expansion is adapted to that of the prosthesis.
  • the dental cavity is first prepared by cutting it by milling and giving it a suitable draft.
  • a paste is then produced, the composition by weight of which is as follows:
  • the dough is made by mixing 65 volumes of filler in 35 volumes of resin.
  • the paste thus obtained is placed in the mouth so as to close the cavity produced in the tooth and the upper part of the paste is given the shape that the prosthesis should have.
  • the photopolymerization is carried out using an ultraviolet lamp.
  • the prosthesis blank thus obtained is removed from the mold, then its thermopolymerization is carried out by heating it for 1 hour at 80 ° C., then for 1 hour at 110 ° C.
  • the sintering is then carried out by bringing the blank to 100 ° C. in 3 hours, which destroys the resin, then to 1120 ° C. in 1 hour, the temperature which is maintained for 2 hours.
  • the glass is then infiltrated, which has the following composition by weight: -If 20% -Al2O3 12% -B2O3 3% -La2O3 40% -TiO2 7% Coloring oxides 2%
  • the prosthesis blank is placed in a cup on the glass powder.
  • the temperature of the oven is brought to 600 ° C. in 6 minutes, the vacuum is produced in the oven and its temperature is raised to 1140 ° C. in 15 minutes, the oven is maintained at 1140 ° C. for 30 minutes and it is cooled in 10 minutes.
  • the prosthesis is then sandblasted to remove excess glass and then polished.
  • the dentist prepares the tooth by cutting it and by milling its perimeter to reduce its height and produce a suitable draft.
  • Such shells are commercially available. They contain for example 80% by weight of MgAl2O4 spinel and 20% by weight of whiskeys (mullite 3Al2O3-2SiO2).
  • the dentist sets up the shell, adapting its shape to the clinical case, either by milling or by adding material using a polymerizable composite.
  • the paste is produced by mixing before use 62, volumes of filler, 38 volumes of resin (constituents A and B equally).
  • the dentist fills the shell with this paste and then places it on the tooth.
  • the prosthetist proceeds to a heat treatment which consists in bringing the temperature of the prosthesis blank to 400 ° C in 6 hours to destroy the resin, then to 1160 ° C in 1 hour 30 minutes. This temperature is held for 2 hours, after which the blank is allowed to cool.
  • the impregnation is carried out as indicated above by bringing the temperature to 700 ° C. in 10 minutes in air, then by vacuuming and by bringing the temperature to 1150 ° C. in 30 minutes and maintaining this temperature for 1 hour. , after which the prosthesis is allowed to cool, which is then polished.
  • the dentist takes an impression of the tooth, then reconstructs its morphology with wax or resin and makes a transparent gutter by thermoforming, then prepares the tooth by milling and gives it the suitable draft.
  • the paste is produced by mixing, before use, 72 volumes of filler with 14 volumes of base paste A and 14 volumes of catalyst B.
  • the dentist then proceeds to the placement on the tooth of the gutter filled with the paste.
  • the chemopolymerization proceeds to demould the prosthesis blank.
  • the prosthetist then proceeds to heat treatment the blank by bringing it to 400 ° C in 5 hours to destroy the resin, then to 1190 ° C in 2 hours, the temperature at which he maintains it for 2 hours.
  • the infrastructure is then impregnated with glass by proceeding as indicated in the previous examples, the glass used has the following composition by weight: -If 15% -B2O3 8% -Al2O3 20% -La2O3 30% -Y2O3 15% -TiO2 8% - Coloring oxides 4%
  • the infiltration is carried out by bringing the blank to 700 ° C. in 6 minutes in air, then by raising the temperature to 1180 ° C. in 20 minutes under vacuum. The temperature is maintained at 1180 ° C for 15 minutes under vacuum and cooled in air to bring it to room temperature in 10 minutes.
  • the excess glass is then removed and polished, and the prosthesis is then fixed by gluing or sealing.
  • the dentist takes the impression of the prepared tooth which is sent to the laboratory.
  • the technician must use a non-shrinkable plaster (less than 0.1%) which can be worn for 2 hours at a temperature of 100 to 120 ° C.
  • a release agent consisting, for example, of non-reactive silicone oil.
  • the prosthetist then fills the inlay cavity on the plaster model using a paste which he prepares and which has the following weight composition:
  • the paste is obtained by mixing 55 volumes of filler with 45 volumes of resin before use.
  • the technician applies the paste and sculpts it.
  • the impregnation is then carried out with a glass having the following weight composition: -If 18% -Al2O3 10% -B2O3 18% -La2O3 30% -Y2O3 15% -TiO2 8% - Coloring oxides 1%
  • Infiltration is carried out by raising the temperature to 650 ° C in 6 minutes in air, then to 1120 ° C in 10 minutes under vacuum. The temperature is maintained at 1120 ° C. under vacuum for 25 minutes, then the prosthesis is cooled in 5 minutes.
  • the prosthetist then proceeds to finish the prosthesis by removing excess glass and performing its polishing.
  • the prosthesis thus obtained is then fixed to the tooth by gluing or sealing.
  • the dentist prepares the tooth by giving it its size and its skin and takes its impression according to the conventional technique.
  • the dental technician makes a model of the tooth with plaster. He applied a spacer varnish to the model and then a release agent consisting of non-reactive silicone oil.
  • thermopolymerizable paste having the following composition by weight:
  • the paste is made just before use by mixing 66 volumes of filler with 34 volumes of resin.
  • the technician After filling the shell with the paste, the technician places it on the model and proceeds to the elimination of excess paste, and to the finishing of the limits.
  • thermopolymerization by heating for one hour at the temperature of 130 ° C., then after demolding, it proceeds to a new heating of one hour at the temperature of 180 ° C.
  • the prosthetist then brings the prosthesis blank to 500 ° C in 8 hours to destroy the resin, then to 1170 ° C in 1 hour, temperature which it maintains for 2 hours, then it allows the prosthesis to cool in the oven.
  • the infrastructure is then, according to the method described above, infiltrated with a glass having the following composition: -If 20% -Al2O3 12% -B2O3 8% -La2O3 45% -Y2O3 5% -TiO2 6% - Coloring oxides 4%
  • the infiltration is carried out by raising its temperature to 600 ° C. for 10 minutes in air, then by bringing it to 1150 ° C. under vacuum in 40 minutes after having maintained the temperature at 1150 ° C. for 30 minutes under vacuum, in let cool.
  • the crown can then be applied by gluing or sealing.
  • An inlay according to the invention is produced by operating as indicated in Example 4, except that a paste having the following weight composition is used:
  • the paste is obtained by mixing 75 volumes of filler with 25 volumes of resin.
  • Thermopolymerization is carried out on the tooth model in an oven for 1 hour at 80 ° C, then for 1 hour at 120 ° C.
  • the sintering is carried out by raising the temperature to 400 ° C. in 3 hours to destroy the resin, then by bringing it to 1060 ° C. in 1 hour. This temperature is then maintained at 1060 ° C for 4 hours and allowed to cool.
  • the prosthetist then checks and if necessary rectifies the infrastructure.
  • the thermal infiltration cycle consists in raising the temperature to 700 ° C in 3 minutes in the presence of air, then in bringing the temperature to 1100 ° C in 15 minutes under vacuum. The temperature is maintained at 1100 ° C. for 12 minutes under vacuum, then the prosthesis is cooled in 8 minutes in air.
  • the technician removes excess glass by sandblasting.
  • the prosthesis is then fixed to the tooth by sealing or gluing.
  • An onlay prosthesis according to the invention is produced by proceeding as indicated in Example 4, except that a paste having the following weight composition is used:
  • the paste is made before use by mixing 65 volumes of filler with 35 volumes of resin.
  • the infrastructure is thermopolymerized on the tooth model in an oven for 1 hour at 100 ° C, then for 1 hour at 120 ° C.
  • sintering is carried out, bringing the temperature to 460 ° C. in 4 hours to destroy the resin, then to 1120 ° C. in 1 hour. The temperature is maintained at 1120 ° C for 2 hours and allowed to cool.
  • the infrastructure is rectified, then, as indicated above, its infiltration with a glass having the following composition by weight -If 80% -B2O3 20% -Al2O3 6% -La2O3 25% -Y2O3 15% -TiO2 4% with a thermal cycle consisting in raising the temperature to 600 ° C in 6 minutes in the presence of air and then bringing the temperature to 1140 ° C in 10 minutes under vacuum. The temperature of 1140 ° C. is maintained under vacuum for 20 minutes, then it is followed by air cooling in 10 minutes.
  • the excess glass is then removed by sandblasting and a volume enameling is carried out with dental ceramic having a coefficient of expansion compatible with that of the prosthesis.
  • a ceramic having the following composition by weight can be used for this purpose: -Sodium oxide 4.5% -Potassium oxide 7.5% - Calcium oxide 1.7% - Aluminum oxide 14% - Silicon oxide 65.3% - Boron oxide 7%
  • the onlay is placed by sealing or gluing.
  • Example 4 To make an inlay according to the invention in the laboratory, the procedure is as indicated in Example 4 by making a paste from:
  • compositions are given by weight.
  • the dough is prepared at the time of use by mixing 70 volumes of filler with 30 volumes of liquid.
  • the inlay is modeled, then dried for 1 hour in an oven at 80 ° C.
  • the infrastructure After demolding, the infrastructure is sintered, bringing it to 500 ° C in 1 hour to destroy the binder, then to 1130 ° C in 1 hour, a temperature which is maintained for 2 hours.
  • Example 4 To make an inlay according to the invention, the procedure is as indicated in Example 4, except that the dough is made from:
  • compositions given above are weight compositions.
  • the paste is produced by mixing just before use 63 volumes of metal oxide filler with 37 volumes of liquid.
  • the liquid can consist of: -Solvent (2/3 ethylene trichlor-1/3 ethanol) 85% - Binder (ethyl cellulose) 15%
  • the blank formed using this paste is dried for 1 hour in an oven at 80 ° C, then demolded.
  • Example 4 To make an onlay according to the invention, the procedure is as indicated in Example 4 but by making up the dough from:
  • the dough is prepared by mixing at the time of use 65 volumes of filler with 35 volumes of liquid.
  • the liquid can be constituted by: -Plasticizer (octyl phthalate) 10% - Organic solvent (mixture of 63% trichlorethylene and 24% ethanol) 87% -binder (polyvinyl butyral) 3%
  • the inlay After modeling the inlay, it is dried for 30 minutes at 80 ° C in an oven.
  • the sintering is carried out by bringing the blank to 450 ° C in 1 hour 30 minutes to destroy the binder, then to 1150 ° C in 1 hour, temperature which is maintained for 2 hours.
  • biocompatible ceramic prostheses are obtained, having a translucency similar to that of the teeth and good mechanical strength.

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  • Health & Medical Sciences (AREA)
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Claims (15)

  1. Verfahren zur Herstellung von keramischen Zahnprothesen mit vergleichbarer durchscheinender Beschaffenheit wie Zahnschmelz, die eine erhöhte mechanische Festigkeit besitzen und bioverträglich sind, wobei das Verfahren dadurch gekennzeichnet ist,
       daß man eine Kunststoffpaste herstellt, die aus einer Mischung aus einem Harz oder organischen Bindemittel mit feinen Teilchen aus Aluminiummagnesiumspinell, Aluminiumoxid und Magnesiumoxid bestehen; daß man der Paste die Form der vorgesehenen Prothese gibt; daß man die Polymerisation das Harzes oder das Abbinden des organischen Bindemittels zur Fixierung der Form der Paste hervorruft; daß man die auf diese Weise in Form gebrachte Paste einer thermischen Behandlung unterwirft, um in einer ersten Stufe die Calcinierung den Harzes oder des Bindemittels und in einer zweiten Stufe die reaktive Sinterung der Teilchen aus dem Aluminiummagnesiumspinell, dem Aluminiumoxid und dem Magnesiumoxid durchführt; daß man gegebenenfalls eine Korrektur der Form des auf diese Weise erhaltenen porösen Unterbaus vornimmt; und daß man eine Infiltration dieses Unterbaus mit Hilfe eines Glases in geschmolzenem Zustand vornimmt.
  2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die Mengen des während der reaktiven Sinterung vorhandenen Aluminiumoxids und Magnesiumoxids so beschaffen sind, daß die Sinterungsbedingungen zur Bildung einer zusätzlichen Menge an Aluminiummagnesiumspinell führen und dabei eine Expansion des Unterbaus hervorrufen, die die Kontraktion aufgrund der Polymerisation oder das Abbindens sowie aufgrund der Calcinierung des Harzes oder des Bindemittels ausgleicht.
  3. Verfahren nach einem der Ansprüche 1 und 2, dadurch gekennzeichnet, daß die Paste mit einem organischen polymerisierbaren Harz, wie einem Polyepoxidharz, einem Polyesterharz oder Vinylesterharz, das während der Calcinierung zerstört wird, gebildet ist.
  4. Verfahren nach Anspruch 3, dadurch gekennzeichnet, daß die Härtung der Paste durch die Polymerisation des Harzes, insbesondere durch Photopolymerisation, chemische Polymerisation oder thermische Polymerisation hervorgerufen wird.
  5. Verfahren nach einem der Ansprüche 1 und 2, dadurch gekennzeichnet, daß es sich beim Bindemittel um ein organisches Bindemittel handelt, das aus einem Celluloseester, wie Methylcellulose, Methylhydroxyethylcellulose, Methylhydroxypropylcellulose, Carboxymethylcellulose oder Hydroxyethylcellulose, einem Natrium- oder Ammoniumalginat, einem löslichen Celluloseether, wie Ethylcellulose oder Celluloseacetat oder aus Polyvinylbutyral besteht, die sich während der Calcinierung zersetzen.
  6. Verfahren nach einem dar Ansprüche 1 bis 5, dadurch gekennzeichnet, daß der anorganische Füllstoff der Paste aus einer Mischung von feinen Teilchen mit einem Gehalt an 50 bis 84 Gew.-% Aluminiummagnesiumspinell, 10 bis 32 Gew.-% Aluminiumoxid und 6 bis 18 Gew.-% Magnesiumoxid besteht.
  7. Verfahren nach einem der Ansprüche 3 und 4, dadurch gekennzeichnet, daß das polymerisierbare Harz 40 bis 90 Gew.-% Polyepoxid-, Polyester- oder Vinylesterharz, 0 bis 80 Gew.-% monomeres reaktives Verdünnungsmittel und 0,5 bis 5 Gew.-% Katalysator, 0 bis 4 Gew.-% Beschleuniger und 0 bis 10 Gew.-% Weichmacher enthält.
  8. Verfahren nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, daß die Metalloxid-Füllstoffteilchen eine Größe von weniger als 40 µm und vorzugsweise von 0,5 µm bis 20 µm aufweisen.
  9. Verfahren nach einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, daß die Paste, der man die Form der Prothese verleiht, 55 bis 78 Vol.-% Metalloxid enthält, wobei der Rest aus dem Harz oder dem Bindemittel besteht.
  10. Verfahren nach einem der Ansprüche 1 bis 9, dadurch gekennzeichnet, daß man der verformbaren Paste die Form der vorgesehenen Prothese verleiht, indem man die im Mund auf einen vorher präparierten Zahn aufbringt.
  11. Verfahren nach einem der Ansprüche 1 bis 9, dadurch gekennzeichnet, daß man der verformbaren Paste die vorgesehene Form der Prothese verleiht, indem man sie auf ein Gipsmodell aufbringt.
  12. Verfahren nach einem der Ansprüche 1 bis 11, dadurch gekennzeichnet, daß man eine bearbeitbare, poröse, keramische Kokille verwendet, um der verformbaren Paste die äußere Form der vorgesehenen Prothese zu verleihen.
  13. Bioverträgliche, keramische Zahnprothese mit einer natürlichem Zahnschmelz ähnlichen durchscheinenden Beschaffenheit und einer erhöhten mechanischen Festigkeit, dadurch gekennzeichnet, daß sie nach einem Verfahren gemäß einem der Ansprüche 1 bis 12 erhalten worden ist und aus einem starren, porösen Unterbau gebildet ist, die durch reaktives Sintern feiner Teilchen aus Aluminiummagnesiumspinell, Aluminiumoxid und Magnesiumoxid erhalten worden ist, wobei die Poren dieses Unterbaus durch ein später bei erhöhter Temperatur infiltriertes Glas besetzt sind.
  14. Prothese nach Anspruch 13, dadurch gekennzeichnet, daß sie im wesentlichen aus 45 bis 70 Gew.-% Aluminiummagnesiumspinell, 8 bis 20 Gew.-% Aluminiumoxid, 3 bis 12 Gew.-% Magnesiumoxid und 20 bis 40 Gew.-% Glas besteht.
  15. Prothese nach einem der Ansprüche 13 und 14, dadurch gekennzeichnet, daß sie mit einem keramischen Material emailliert ist, dessen Ausdehnungskoeffizient an den der Prothese angepaßt ist.
EP92923838A 1991-10-15 1992-10-15 Vollkeramische dentalprothese aus aluminiumoxyd/magnesiumoxyd spinell enthaltend keramik und verfahren zu seiner herstellung Expired - Lifetime EP0563372B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR9112673A FR2682297A1 (fr) 1991-10-15 1991-10-15 Prothese dentaire entierement ceramique a base de spinelle alumine/magnesie et son procede de fabrication.
FR9112673 1991-10-15
PCT/FR1992/000974 WO1993007846A1 (fr) 1991-10-15 1992-10-15 Prothese dentaire entierement ceramique a base de spinelle alumine/magnesie et son procede de fabrication

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EP0563372A1 EP0563372A1 (de) 1993-10-06
EP0563372B1 true EP0563372B1 (de) 1995-11-22

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EP (1) EP0563372B1 (de)
JP (1) JPH06503501A (de)
AT (1) ATE130508T1 (de)
AU (1) AU2947492A (de)
CA (1) CA2098388A1 (de)
DE (1) DE69206256T2 (de)
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WO (1) WO1993007846A1 (de)

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JPH06503501A (ja) 1994-04-21
DE69206256T2 (de) 1996-07-25
FR2682297B1 (de) 1995-06-02
DE69206256D1 (de) 1996-01-04
EP0563372A1 (de) 1993-10-06
AU2947492A (en) 1993-05-21
US5447967A (en) 1995-09-05
ATE130508T1 (de) 1995-12-15
CA2098388A1 (fr) 1993-04-16
FR2682297A1 (fr) 1993-04-16
WO1993007846A1 (fr) 1993-04-29

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